A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1941n223



Internal ID22804909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83501101..83543700hg38UCSC Ensembl
chr13:84075236..84117835hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3842600
hg1942600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6494583, nsv6482327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1941n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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